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Absorbance
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===Method of measurement=== Typically, absorbance of a dissolved substance is measured using [[absorption spectroscopy]]. This involves shining a light through a solution and recording how much light and what wavelengths were transmitted onto a detector. Using this information, the wavelengths that were absorbed can be determined.<ref>{{cite web|last1=Reusch|first1=William|title=Visible and Ultraviolet Spectroscopy|url=https://www2.chemistry.msu.edu/faculty/reusch/virttxtjml/Spectrpy/UV-Vis/spectrum.htm|access-date=2014-10-29}}</ref> First, measurements on a "blank" are taken using just the solvent for reference purposes. This is so that the absorbance of the solvent is known, and then any change in absorbance when measuring the whole solution is made by just the solute of interest. Then measurements of the solution are taken. The transmitted spectral radiant flux that makes it through the solution sample is measured and compared to the incident spectral radiant flux. As stated above, the spectral absorbance at a given wavelength is <math display="block">A_\lambda = \log_{10}\!\left(\frac{\Phi_{\mathrm{e},\lambda}^\mathrm{i}}{\Phi_{\mathrm{e},\lambda}^\mathrm{t}}\right)\!.</math> The absorbance spectrum is plotted on a graph of absorbance vs. wavelength.<ref>{{cite web|last1=Reusch|first1=William|title=Empirical Rules for Absorption Wavelengths of Conjugated Systems|url=https://www2.chemistry.msu.edu/faculty/reusch/virttxtjml/Spectrpy/UV-Vis/uvspec.htm#uv1|access-date=2014-10-29}}</ref> An [[Ultraviolet-visible spectroscopy#Ultraviolet–visible spectrophotometer]] will do all this automatically. To use this machine, solutions are placed in a small [[cuvette]] and inserted into the holder. The machine is controlled through a computer and, once it has been "blanked", automatically displays the absorbance plotted against wavelength. Getting the absorbance spectrum of a solution is useful for determining the concentration of that solution using the Beer–Lambert law and is used in [[HPLC]].
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